Pharmaceutical compositions comprising an oligonucleotide as an active agent
A pharmaceutical composition is disclosed, which composition comprises an oligonucleotide as an active agent, the oligonucleotide being adapted to target nucleic acids encoding CD40 thereby to modulate the expression of CD40 in mammalian cells, and a liposome as an excipient. Said liposome is an amphoteric liposome. Also disclosed is a method for the treatment or prophylaxis of a disease or condition associated with the expression of CD40 in a human or non-human animal patient by administering to said patient a therapeutically or prophylactically effective amount of such a composition.
1 . A pharmaceutical composition comprising an oligonucleotide as an active agent, said oligonucleotide adapted to target nucleic acids encoding CD40 so as to modulate the expression of CD40 in mammalian cells, and an amphoteric liposome as an excipient.
2 . The pharmaceutical composition according to claim 1 , wherein said liposome has an isoelectric point of between 4 and 7.4.
3 . The pharmaceutical composition according to claim 1 , wherein said amphoteric liposome is negatively charged or neutral at pH 7.4 and cationic at pH 4.
4 . The pharmaceutical composition according to claim 1 , wherein said amphoteric liposome is formed from a lipid phase comprising an amphoteric lipid.
5 . The pharmaceutical composition according to claim 4 , wherein said lipid phase comprises 5 to 30 mol. % of said amphoteric lipid.
6 . The pharmaceutical composition according to claim 4 , wherein said amphoteric lipid is selected from the group consisting of HistChol, HistDG, isoHistSuccDG, Acylcarnosin and HCCHol.
7 . The pharmaceutical composition according to claim 1 , wherein said amphoteric liposome is formed from a lipid phase comprising a mixture of lipid components with amphoteric properties.
8 . The pharmaceutical composition according to claim 7 , wherein said mixture of lipid components comprises anionic or cationic components and wherein at least one of the components is pH responsive.
9 . The pharmaceutical composition according to claim 8 , wherein said mixture of lipid components comprises (i) a stable cationic lipid and a chargeable anionic lipid, (ii) a chargeable cationic lipid and chargeable anionic lipid or (iii) a stable anionic lipid and a chargeable cationic lipid.
10 . The pharmaceutical composition according to claim 9 , wherein said lipid components comprise one or more anionic lipids selected from the group consisting of DGSucc, DMPS, DPPS, DOPS, POPS, DMPG, DPPG, DOPG, POPG, DMPA, DPPA, DOPA, POPA, CHEMS and Cetyl-P.
11 . The pharmaceutical composition according to claim 9 , wherein said lipid components comprise one or more anionic lipids selected from the group consisting of DGSucc, DOPA, CHEMS and Cetyl-P.
12 . The pharmaceutical composition according to claim 8 , wherein said lipid components comprise one or more cationic lipids selected from the group consisting of DMTAP, DPTAP, DOTAP,DC-Chol, MoChol, HisChol, DPIM, CHIM, DORIE, DDAB,DAC-Chol, TC-Chol, DOTMA, DOGS, (C18) 2 Gly + N,N-dioctadecylamido-glycin, CTAP, CPyC, DODAP and DOEPC.
13 . The pharmaceutical composition according to claim 8 , wherein said lipid components comprise one or more cationic lipids selected from the group consisting of DOTAP, DC-Chol, MoChol and HisChol.
14 . The pharmaceutical composition according to claim 4 , wherein said lipid phase further comprises a neutral phospholipid.
15 . The pharmaceutical composition according to 14 , wherein said lipid phase comprises a neutral phosphatidylcholine.
16 . The pharmaceutical composition according to claim 15 , wherein said phosphatidylcholine is selected from the group consisting of DMPC, DPPC, DSPC, POPC, DOPC, natural source phosphatidylcholines, soy bean PC and egg PC.
17 . The pharmaceutical composition according to claim 15 , wherein said neutral phosphatidylcholine is selected from the group consisting of POPC, natural or hydrogenated soy bean PC, natural or hydrogenated egg PC, DMPC, DPPC and DOPC.
18 . The pharmaceutical composition according to claim 15 , wherein said phosphatidylcholine comprises POPC, non-hydrogenated soy bean PC, or non-hydrogenated egg PC.
19 . The pharmaceutical composition according to claim 15 , wherein said lipid phase comprises at least 15 mol. % of said phosphatidylcholine.
20 . The pharmaceutical composition according to claim 19 , wherein said lipid phase comprises about 60 mol. % POPC, about 10 mol. % DOTAP and about 30 mol. % CHEMS.
21 . The pharmaceutical composition according to claim 14 , wherein said neutral lipid comprises a phosphatidylethanolamine.
22 . The pharmaceutical composition according to claim 21 , wherein said phosphatidylethanolamine is selected from DOPE, DMPE, or DPPE.
23 . The pharmaceutical composition according to claim 21 , wherein said lipid phase comprises at least 20 mol. % of phosphatidylcholine and phosphatidylethanolamine.
24 . The pharmaceutical composition according to claim 21 , wherein said lipid phase comprises a mixture of anionic and cationic lipids with amphoteric properties, phosphatidylcholine and phosphatidylethanolamine.
25 . The pharmaceutical composition according to claim 24 , wherein said cationic lipid comprises MoChol and said anionic lipid comprises CHEMS or DMG-Succ.
26 . The pharmaceutical composition according to claim 25 , wherein said lipid phase comprises:
(a) about 15 mol. % POPC, about 45 mol. % DOPE, about 20 mol. % MoChol and about 20 mol. % CHEMS;
(b) about 10 mol. % POPC, about 30 mol. % DOPE, about 30 mol. % MoChol and about 30 mol. % CHEMS;
(c) about 10 mol. % POPC, about 30 mol. % DOPE, about 20 mol. % MoChol and about 40 mol. % CHEMS; or
(d) about 6 mol. % POPC, about 24 mol. % DOPE, about 47 mol. % MoChol and about 23 mol. % CHEMS.
27 . The pharmaceutical composition according to claim 21 , wherein said lipid phase comprises DOPE and POPC.
28 . The pharmaceutical composition according to claim 14 , wherein said lipid phase further comprises cholesterol.
29 . The pharmaceutical composition according to claim 28 , wherein said lipid phase comprises from 30 mol. % to 50 mol. % cholesterol.
30 . The pharmaceutical composition according to claim 28 , wherein said lipid phase comprises about 30 mol. % POPC, about 10 mol. % DOTAP, about 20 mol. % CHEMS and about 40 mol. % Chol.
31 . The pharmaceutical composition according to claim 28 , wherein said lipid phase comprises about 60 mol. % POPC, about 20 mol. % HistChol and about 20 mol. % Chol.
32 . The pharmaceutical composition according to claim 23 , wherein said composition further comprises a vehicle and is formulated for systemic delivery.
33 . The pharmaceutical composition according to claim 1 , wherein said composition further comprises a vehicle and is formulated for local administration.
34 . The pharmaceutical composition according to claim 1 , wherein said liposome has a size in the range 50 to 500 nm.
35 . The pharmaceutical composition according to claim 1 , wherein said oligonucleotide is an antisense oligonucleotide of 15 to 50 basepairs in length.
36 . The pharmaceutical composition according to claim 35 , wherein said oligonucleotide contains phosphothioate linkages, 2′MOE modified nucleobases, LNA nucleobases, FANA nucleobases, naturally occurring ribonucleotides, or naturally occurring deoxyribonucleotides.
37 . The pharmaceutical composition according to claim 1 , wherein said oligonucleotide comprises a siRNA of 15 to 50 basepairs in length.
38 . The pharmaceutical composition according to claim 1 , wherein said oligonucleotide targets the human CD40 gene.
39 . A method of treating or preventing an inflammatory, immune or autoimmune disorder, comprising administering to a recipient in need thereof, the pharmaceutical composition according to claim 1 in an amount effective to treat or prevent the condition.
40 . A method of treating or preventing a disease or condition selected from graft rejection, graft-versus-host disease, multiple sclerosis, systemic lupus erythematosous, rheumatoid arthritis, asthma, inflammatory bowel disease, psoriasis, or thyroiditis, comprising administering to a recipient in need thereof, the pharmaceutical composition according to claim 32 in an amount effective to treat or prevent the disease or condition.
41 . A method of treating or preventing a disease or condition selected from graft rejection, graft-versus-host disease, inflammatory bowel disease, Morbus Crohn, or Colitis ulcerosa, comprising administering to a recipient in need thereof, the pharmaceutical composition according to claim 33 in an amount effective to treat or prevent the disease or condition.
42 . The method according to claim 39 , wherein the recipient is a human or non-human animal.
43 . The method according to claim 40 , wherein the recipient is a human or non-human animal.
44 . The method according to claim 41 , wherein the recipient is a human or non-human animal.